In-House Clinical Research Associate (CRA)
$75k - $95kPraxis
Position Summary We are seeking an In-House Clinical Research Associate (CRA) who’s excited to help execute fast, high-quality clinical trials that drive our mission forward. You’ll be a key player in ensuring our studies are inspection-ready, patient-centric, and run with rigor. This role supports both internal team coordination and site-facing execution—keeping timelines sharp, data clean, and communication clear. Primary Responsibilities Support study execution by managing meeting logistics, documenting decisions, and tracking action items. Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards are met. Responsible for filing the site-level documents into the Trial Master Files ( TMFs) in a timely manner. Track, review, and organize essential documents from sites and vendors. Identify, escalation, and help resolve site-level issues in collaboration with cross‑functional teams. Assist with regulatory submissions and other study deliverables. Drive process improvements that enhance speed, quality, and patient impact. Qualifications and Key Success Factors Bachelor’s degree in a life science or health‑related field, or equivalent industry experience. 5+ years of clinical trial experience in biotech, pharma, or CRO settings. Solid knowledge of GCP, ICH guidelines, and regulatory requirements. Exceptional organizational and communication skills. A proactive, problem‑solving mindset with high attention to detail. Comfortable managing multiple priorities in a fast‑paced, mission‑driven environment. Strong team player who thrives in flat, agile organizations. Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). Compensation & Benefits At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world‑class benefits package to help you thrive. Thinking about the future? We match dollar‑for‑dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long‑term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays, and company‑wide shutdowns. Not to mention, you’ll also be joining a phenomenal crew of colleagues who are smart, engaged, and inspiring. We aim high, collaborate hard, and produce results. Let’s achieve the impossible together! 99% of the premium paid for medical, dental, and vision plans. company‑paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. match dollar‑for‑dollar up to 6% on eligible 401(k) contributions. long‑term stock incentives and ESPP. discretionary quarterly bonus. extremely flexible wellness benefit. generous PTO. paid holidays.company‑wide shutdowns. Annualized Base Salary $75,000 — $95,000 USD Company Overview Praxis Precision Medicines is a clinical‑stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high‑impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust , Ownership , Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members. Diversity, Equity & Inclusion Diversity, Equity & Inclusion Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE ® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr Praxis
$96.2k - $151.4k
...phases of the trial. Performs clinical study site management/... ...Protocol, Site Monitoring Plan and associated documents. Gains an in-depth... ...problems and escalates per defined CRA Escalation Pathway as... ...them to develop strong clinical research capabilities. Travel Requirements...SuggestedFor contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week- ...Overview Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced...SuggestedRemote work
- ...DallasThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality...SuggestedFull timeRemote work
$38 - $40 per hour
...job poster from Baim Institute for Clinical Research Director, Human Resources at Baim... ...The Sr. Clinical Research Associate/Field Monitor Contractor performs... ...resolution, collaborate with in-house Clinical Research Associate (CRA) team, ensuring regulatory documents...HousePart timeFor contractorsInterim roleRemote workWork from home10 hours per week- ...ClinChoice is a global, full-service CRO providing clinical research services to pharmaceutical, biotechnology, medical device... ...seeking an experienced Senior Clinical Research Associate (Senior CRA) to join our in-house team. As a Senior CRA, you will manage 2–3 clinical...HousePermanent employmentContract workFor contractorsFreelanceWork at officeLocal areaRemote work
- ...Alcedis is a well-established and successful clinical research organization headquartered in Germany,... ...for experienced Clinical Research Associates (CRAs) to join our U.S.-based expert network... ...as a Clinical Research Associate (CRA) / Clinical Monitor ~ Experience in GCP...Full timePart timeRemote work
$125k - $140k
...Oncology Sr. CRA 2 Our FSP team is currently seeking an Oncology... ...your skills, knowledge, and clinical judgement to provide a high standard... ...based upon clinical research standards. Responsibilities... ...computer software developed both in-house and off-the-shelf. Light to...HouseWork at officeLocal areaNight shift$97k - $193k
...quality and excellence. We are Worldwide Clinical Trials, and we are a global team of... ...the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself... ...regulatory submissions, TMF management, and in‑house CRAs for projects with heavy site...HouseHourly payWork at officeRemote workWorldwide$71.9k - $169.3k
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...to patients faster.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the...Full timePart timeImmediate startWorldwide- ...Pulse Biosciences is seeking a Senior Clinical Research Associate to manage and monitor soft tissue ablation trials in the U.S. remote setup. The Sr. CRA will support study planning, site startup, patient recruitment, data quality, and regulatory compliance with CFR FDA...Remote work
- ...Syneos Health, Inc. is seeking a CRA II/Sr CRA for Germany (remote across Leipzig/Halle/Berlin) to monitor clinical sites. The role requires fluency in German and English, good regulatory knowledge, and the ability to manage remote and on-site visits. You will perform...Remote work
- ...with a leading Cardiovascular Medical Device company that is seeking an experienced Clinical Research Associate Contractor on a remote basis. Key Requirements Proven experience as a CRA within the cardiovascular medical device field. Strong knowledge of FDA regulations...Contract workFor contractorsFreelanceImmediate startRemote work
$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry... ...permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and metabolic studies...Permanent employmentRemote work- ...Syneos Health, Inc. is seeking a Clinical Monitoring/CRA to support site management, monitoring, and data integrity across sponsor studies in a remote setup. The role emphasizes regulatory compliance and collaboration with cross-functional teams. The position requires...Remote work
- ...Syneos Health is seeking a CRA II for sponsor-dedicated oncology/neurology work (home-based in GA/SC). The role involves site qualification, monitoring, data review, and regulatory compliance across real-world late-phase studies. Travel up to 30% is required, with on-site...Remote workWork from home
- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization... ...training as required. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research AssociateThis role is located in either New York or New Jersey.The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in...Hourly payTemporary workLocal areaRemote work
- ...Syneos Health in Germany is seeking a CRA I to join our clinical solutions team. This role supports site qualification, initiation, monitoring, and close-out visits, performed on-site or remotely, to ensure regulatory and ICH-GCP compliance. You will verify informed consent...Remote work
$4,000 - $9,000 per month
...Clinical Research AssociateDotLab is transforming the diagnosis and management of endometriosis... ....DotLab is seeking a Clinical Research Associate to join our team and support DotLab clinical... ...required.2+ years of study monitoring (CRA) experience; 1+ years of study...Work at officeRemote workWorldwideFlexible hours$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the...Permanent employmentWork at officeRemote work$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...Contract workRemote workNight shift- ...Syneos Health in the Paris area is seeking a Senior CRA I in Oncology to monitor clinical sites for sponsor-led trials. This role combines on-site and remote activities to ensure protocol adherence and data integrity across study sites. You will perform site qualification...Remote work
- ...Parexel International is seeking an FSP CRA with 3+ years of CRA experience from Australia or New Zealand. The position is based in NSW or VIC and focuses on overseeing site monitoring and study conduct. You will manage site activation through database lock, coach site...
- ...growing organization who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires limited to no travel... ...recommend qualified sites. Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites...Interim role
- ...Worldwide Clinical Trials seeks a Senior Clinical Research Associate (CNS) to support Midwest and Southeast regions with remote options. You will lead site management... ...compliance. Ideal candidates have 5+ years as a CRA, a 4-year degree or nursing degree, and strong...Remote workWorldwide
- ...applications and next steps. Our partner is looking for a Sr Clinical Research Associate based in United States. This role offers an opportunity... .... Assist with the preparation and delivery of CRA, departmental, and sponsor-specific training and presentations...Temporary workWork at officeLocal areaRemote workFlexible hours
- ...Clinical Research Associate - Northeast ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to... ...mission to shape the future of clinical development. As a CRA I at ICON, you will contribute to our clinical trial...Flexible hours
- ...Sr CRA or CRA PositionWe are looking for a Sr CRA or a CRA with experience working in... ...to Ethic Submissions experience.Monitors clinical trials and observational studies ensuring... ...negotiations with Sites, Foundations, and local Research & Development Departments in...Contract workWork at officeLocal areaRemote work
- ...Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to oversee research activities at sites involved in our clinical trials across multiple therapeutic areas. You will ensure regulatory compliance, training, and data integrity throughout the study...Worldwide
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX)ICON is a global healthcare intelligence and clinical research organisation... ....2-5 years clinical monitoring experience required (CRA 2 for sponsor)5+ years clinical monitoring experience required...Work experience placementLocal areaWork visa
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